Chronic Illness and the Holidays
- Missing out on fun and events to rest and take care of myself
- Navigating the dreaded “how are you?” or “what are you up to?” questions from family and friends
- Dealing with the judgmental reactions of others when I need to make accommodations for my health (turning down the lights, opening the windows, dietary restrictions, etc.)
- Worrying I will have a flare-up and knowing how hard it will be
- Having to explain to family members why I’m not feeling well
- Responding to unsolicited advice
- Managing the expectations of others
- Being misunderstood and judged by family
- Explaining the unpredictability and irregularity of my symptoms to people who just don’t “get it” — helping them to understand why sometimes I am “OK” and sometimes I am not
- Keeping my nervous system calm and grounded when others’ energies are swirling around me
- Disappointing family by not being able to do the things I used to be able to do
- Missing out on holiday events because of a flare-up or bad migraine attack
- Dealing with family members who don’t understand or respect why I need to take breaks or rest
- Feeling pressure to match the stereotype of partying on New Year’s Eve and knowing my body cannot handle that right now
- Feeling FOMO and overstimulation at the same time
- Handling the way social anxiety manifests in my body
- Not being able to make it to all of the things I want to attend
- Explaining to people that most of my days have both good and bad moments, and that both are legitimate
- Answering questions from family at Christmas about my health
- People judging the legitimacy of my pain when I do show up
- Feeling like I’m a drain on my family and friends because I am sick
- Not making it to special occasions
- Pacing myself for events
- Wondering if people will think I am “faking it” because I can hide my symptoms so well
- Feeling like I am a burden to those around me
- A flare-up striking at the wrong time and missing time with family and friends
- Feeling out of it and not like myself with family when I have to take extra medication
- Having to explain why I need to lay down or take breaks in the middle of events
- Managing anxiety about extended periods of time out of the house
- People pressuring me to drink alcohol at parties when I can’t (or choose not to) because of my health
- Answering questions about health, school or work
- Having a health crisis spurred by trying to do too much
- Getting a flare-up while traveling or having something happen on the airplane
- Anxiety about when (or what) the next attack of sickness will be
- Family tension that kicks up my pain
- Lowering unrealistic expectations I place on myself
- Advocating for my needs when it is uncomfortable to do so
- Accepting there is a difference between how much I can push myself and how much I should push myself
- Being able to show up for the people I love in the way I want to
- How to manage an attack when I am not at home
- Getting sick on a long car ride and being trapped
- Questions about my health from relatives, how to answer when their inquiries as to why I’m not “better yet”
- Sticking to dietary protocols during events
- Feeling like I am taking too much medication
- Handling sensory overload from crowds, bright lights and music
- Comparing what I can do to what others can do
- Imposing unrealistic expectations on myself just because it is “the holidays”
- People assuming I’m not trying hard enough to get well because I’m still sick
- Explaining to friends back home that I’m not up to seeing them
- Feeling like I am not enough
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